A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891274



Internal ID22666310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52901910..52922349hg38UCSC Ensembl
chr6:52766708..52787147hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3820440
hg1920440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429895
Samples
Known GenesGSTA3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891274
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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